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Question
Why is the coding sequence of an enzyme β-galactosidase a preferred selectable marker in comparison to the ones named above?
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Solution 1
The gene for the enzyme β-galactosidase is an alternative selectable marker. When the foreign gene is inserted within the β-galactosidase gene, the enzyme β- galactosidase gets inactivated. Then the bacteria are grown on a chromogenic substrate. Non-recombinants will produce blue-coloured colonies, while recombinants will produce colourless colonies.
Solution 2
The coding sequence of the enzyme β-galactosidase is a preferred selectable marker compared to antibiotic resistance markers like those in pBR322 because it simplifies the identification of recombinants. Antibiotic-based selection is cumbersome as it requires plating on multiple antibiotic-containing media. In contrast, insertional inactivation of β-galactosidase allows differentiation based on colour. When recombinant DNA is inserted within the β-galactosidase gene, it inactivates the enzyme, resulting in colourless colonies on media with a chromogenic substrate, while non-recombinants produce blue colonies. This visual distinction makes β-galactosidase an efficient and convenient selectable marker for identifying transformants.
RELATED QUESTIONS
How does the β-galactosidase coding sequence act as a selectable marker? Why is it a preferred selectable marker to antibiotic resistance genes? Explain.
Which of the following is correctly matched?
A suitable vector for gene cloning in higher organism is ______.
Plasmids are suitable vectors for gene cloning because these ______.
A cloning vector should possess which of the following characters?
- Origin of replication (Ori)
- Ability to destroy the alien DNA
- Cloning site to link the alien DNA
- The tumour inducing plasmid Ti.
- Selectable marker.
- Low molecular weight
The CORRECT combination is
Plasmid pBR322 has a PstI restriction enzyme site within gene ampR that confers ampicillin resistance. If this enzyme is used for inserting a gene for β-galactoside production and the recombinant plasmid is inserted in an E.coli strain.
What does ‘competent’ refer to in competent cells used in transformation experiments?
A plasmid without a selectable marker was chosen as vector for cloning a gene. How does this affect the experiment?
Describe the role of CaCl2 in the preparation of competent cells?
The following diagram showing restriction sites in E. coli cloning vector pBR322. Find the role of ‘X’ and ‘Y’ genes:

